We have had a long standing interest in the maturation of respiratory control in early life. In particular, we have focussed on the study of mechanisms that can lead to apnea, hypoventilation and hypoxia, conditions that contribute in major ways to morbidity and mortality in infants and children. Although we and others have previously described the ventilatory response to hypoxia in newborns and with maturation, to date, little is known about the cellular and subcellular mechanisms by which graded hypoxia act in the CNS and more specifically in the brainstem. Using intracellular techniques and a brainstem slice preparation, we specifically intent to 1) study the postnatal maturation of the electrophysiologic response to medullary neurons (ventral Nucleus Tractus Solitarius, V-NTS, and Hypoglossal, HYP) to hypoxia in the first several weeks of life in the rat, 2) determine the basic ionic mechanisms that underlie the neuronal excitability during hypoxia and 3) determine whether the electrophysiologic changes seen with hypoxia are mediated by neurotransmitters released by hypoxia. The variables studies will include active and passive cellular properties and membrane properties using current and voltage clamp techniques. In addition, we will use pharmacologic manipulations (e.g., blockers such as TEA, apamin, Cobolt, TTX) ion substitutions (e.g. choline) and ion-selective electrodes to measure changes in ion fluxes (K+, H+) in both intracellular and extracellular compartments. A number of neurotransmitter blockers including Aminophosphonovalerate, Bicuculline, Naloxone and Theophylline will also be used to see whether the electrophysiologic changes seen during hypoxia are neurotransmitter-regulated. Our preliminary results, showing major differences in hypoxic responsiveness between newborns and adults, are very encouraging. We believe that these studies are essential for our understanding of 1) the effects of hypoxia on the function of medullary respiratory-related neurons and 2) neuronal resistance or susceptibility to hypoxic injury in newborns and adults.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD015736-11
Application #
3313218
Study Section
Respiratory and Applied Physiology Study Section (RAP)
Project Start
1981-07-01
Project End
1994-08-31
Budget Start
1991-09-01
Budget End
1992-08-31
Support Year
11
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Yale University
Department
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
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Bevensee, M O; Cummins, T R; Haddad, G G et al. (1996) pH regulation in single CA1 neurons acutely isolated from the hippocampi of immature and mature rats. J Physiol 494 ( Pt 2):315-28
Krishnan, S N; Desai, T; Ward, D C et al. (1995) Isolation and chromosomal localization of a human ATP-regulated potassium channel. Hum Genet 96:155-60
O'Reilly, J P; Jiang, C; Haddad, G G (1995) Major differences in response to graded hypoxia between hypoglossal and neocortical neurons. Brain Res 683:179-86
Krishnan, S N; Haddad, G G (1995) Cloning of glucose transporter-3 (GLUT3) cDNA from rat brain. Life Sci 56:1193-7
Xia, Y; Warshaw, J B; Haddad, G G (1995) Chronic hypoxia causes opposite effects on glucose transporter 1 mRNA in mature versus immature rat brain. Brain Res 675:224-30
Xia, Y; Haddad, G G (1994) Postnatal development of voltage-sensitive Na+ channels in rat brain. J Comp Neurol 345:279-87
Jiang, C; Haddad, G G (1994) Oxygen deprivation inhibits a K+ channel independently of cytosolic factors in rat central neurons. J Physiol 481 ( Pt 1):15-26
Friedman, J E; Haddad, G G (1994) Removal of extracellular sodium prevents anoxia-induced injury in freshly dissociated rat CA1 hippocampal neurons. Brain Res 641:57-64
Jiang, C; Cummins, T R; Haddad, G G (1994) Membrane ionic currents and properties of freshly dissociated rat brainstem neurons. Exp Brain Res 100:407-20

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